Canonical Allele Identifier: CA1616385071
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1761667452

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24204553_24204581del , CM000668.2:g.24204553_24204581del GRCh38
NC_000006.11:g.24204781_24204809del , CM000668.1:g.24204781_24204809del GRCh37
NC_000006.10:g.24312760_24312788del NCBI36
NG_012829.1:g.158473_158501del
NG_012829.2:g.183713_183741del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1023+422_1023+450del MANE Select ENSP00000367715.3:n.1023+422_1023+450del
ENST00000378450.6:c.282+422_282+450del ENSP00000367711.3:n.282+422_282+450del
ENST00000378454.7:c.1023+422_1023+450del ENSP00000367715.3:n.1023+422_1023+450del
NM_001195610.1:c.1023+422_1023+450del NP_001182539.1:n.1023+422_1023+450del
NM_016356.4:c.1023+422_1023+450del NP_057440.2:n.1023+422_1023+450del
NM_016356.5:c.1023+422_1023+450del MANE Select NP_057440.2:n.1023+422_1023+450del
NM_001195610.2:c.1023+422_1023+450del NP_001182539.1:n.1023+422_1023+450del